About this trial
Current treatment guidelines recommend ursodeoxycholic acid (UDCA) as the first-line treatment for new-diagnosed primary biliary cholangitis (PBC) patients. However, up to 40% patients are insensitive to UDCA monotherapy, and evaluation of UDCA response at 12 months may result in long period of ineffective treatment. We aimed to develop a new criterion to reliably identify non-response patients much earlier. Recently, our team designed and validated a new early criterion for distinguishing high-risk PBC patients in a Chinese population for the first time. Our data indicated that PBC patients with ALP ≤ 2.5 × ULN, AST ≤ 2 × ULN, and TBIL ≤ 1 × ULN (Xi'an criterion) after 1 month UDCA treatment were likely to have better prognosis. It can be readily applied in the rapid identification of PBC patients who require additional therapeutic approaches. However, whether it is reasonable to apply it to the response definition of clinical research, and the guidance of PBC management and choice of second-line treatment, further research is needed.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Must have provided written informed consent;
Age 18-75 years;
BMI 17-28 kg/m2
History of AP above ULN for at least six months;
Disqualifiers
History or presence of other concomitant liver diseases.
ALT/AST > 5×ULN, TBIL > 3×ULN.
If female: known pregnancy, or has a positive urine pregnancy test (confirmed by a positive serum pregnancy test), or lactating.
Allergic to fenofibrate or ursodeoxycholic acid.
Trial design
Parallel
Treatments tested in this trial
Placebo Combined With Ursodeoxycholic Acid
Drug1 tablet/ day
Fenofibrate Combined With Ursodeoxycholic Acid
Drug200 mg/day
Treatment groups
Trial outcomes
Primary outcomes
Percentage of patients with complete biochemical response
The normalisation of Alkaline Phosphatase (ALP) and total bilirubin (TBIL).
Secondary outcomes
Percentage of patients having complete biochemical response
The normalisation of Alkaline Phosphatase (ALP) and total bilirubin (TBIL) at 4, 12, 24, and 36 weeks.
Assessment of the fatigue and the quality of life
Change from baseline in primary biliary cholangitis -40 (PBC-40) quality of life (QoL) questionnaire scores.
Assessment of the fatigue and the quality of life
Change from baseline in pruritus as assessed by Visual Analogue Scale (VAS) total score for fatigue and pruritus.
Evolution of the biological markers of the hepatic function or being in the usual prognostic scores
Mayo score at 4, 12, 24, 36, and 48 weeks
Sponsors and contacts
Click on the lead sponsor to view all of their trials.